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后尿道瓣膜患者的终末期肾脏疾病长期风险。

Long-term risk of end stage renal disease in patients with posterior urethral valves.

机构信息

Department of Pediatric Surgery, Hyvinkää Hospital, Hyvinkää, Finland.

出版信息

J Urol. 2011 Dec;186(6):2392-6. doi: 10.1016/j.juro.2011.07.109. Epub 2011 Oct 20.

Abstract

PURPOSE

Congenital obstructive uropathy can lead to end stage renal disease. Progression to end stage renal disease in childhood is well described but long-term prognosis in adulthood has not been thoroughly investigated. In this study we evaluated the risk of end stage renal disease in patients with posterior urethral valves.

MATERIALS AND METHODS

During 1953 to 2003 a total of 200 male patients were treated for posterior urethral valves at our institution and of these 193 could be followed for renal outcome. Followup data on patients treated with dialysis or kidney transplantation were collected from patient records and the Finnish Kidney Transplantation Registry, and data on deceased patients were collected from hospital records and the Finnish Population Register Centre.

RESULTS

Median patient age at evaluation was 31 years (range 6 to 69). Of the 193 patients followed 44 (22.8%) had progression to end stage renal disease. According to a Kaplan-Meier analysis the lifetime risk of end stage renal disease was 28.5% (SE 3.8%). No patient had end stage renal disease after the age of 34 years. The lowest serum creatinine value during postoperative year 1 was associated with speed of progression to end stage renal disease. Early presentation, pneumothorax, bilateral vesicoureteral reflux and recurrent urinary tract infections after the abolition of urethral obstruction were associated with an increased risk of end stage renal disease at followup.

CONCLUSIONS

Congenital obstructive uropathy can lead to end stage renal disease during childhood or young adulthood. However, the risk of end stage renal disease seems to decrease eventually. Poor kidney function at presentation is associated with worse renal prognosis.

摘要

目的

先天性尿路梗阻可导致终末期肾病。儿童期进展为终末期肾病已有充分描述,但成人的长期预后尚未得到彻底研究。本研究评估了后尿道瓣膜患者发生终末期肾病的风险。

材料和方法

1953 年至 2003 年期间,我院共治疗了 200 例男性后尿道瓣膜患者,其中 193 例可随访肾脏结局。通过患者病历和芬兰肾脏移植登记处收集接受透析或肾移植治疗的患者的随访数据,通过医院病历和芬兰人口登记中心收集死亡患者的数据。

结果

评估时患者的中位年龄为 31 岁(范围 6 至 69 岁)。在随访的 193 例患者中,44 例(22.8%)进展为终末期肾病。根据 Kaplan-Meier 分析,终生发生终末期肾病的风险为 28.5%(SE 3.8%)。34 岁后无患者发生终末期肾病。术后第 1 年血清肌酐值最低与进展为终末期肾病的速度有关。早期出现、气胸、双侧输尿管反流和尿道梗阻解除后反复尿路感染与随访时终末期肾病风险增加相关。

结论

先天性尿路梗阻可导致儿童期或青年期发生终末期肾病。然而,终末期肾病的风险最终似乎会降低。就诊时肾功能较差与肾脏预后较差相关。

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